Prenatal diagnosis of holoprosencephaly in two fetuses with der (7)t(1;7)(q32;q32)pat inherited from the father with double translocations

Prenatal Diagnosis

Volumn 23, Issue 2, 2003, Pages 134-137

  Chuang, Louise ^a   Kuo, Pao Lin ^a   Yang, Hsiao Bai ^a,b   Chien, Chung Ho ^a   Chen, Pei Yi ^a   Chang, Chiung Hsin ^a   Chang, Fong Ming ^a  

^a NATIONAL CHENG KUNG UNIVERSITY HOSPITAL   (Taiwan)

^b Ton Yen General Hospital   (Taiwan)

Author keywords

Double translocations; Holoprosencephaly; Partial deletion 7q; Partial duplication 1q; Prenatal diagnosis

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME DELETION; CHROMOSOME TRANSLOCATION; CYTOGENETICS; FACE DYSMORPHIA; FEMALE; FETUS; HOLOPROSENCEPHALY; HUMAN; KARYOTYPE; KARYOTYPE 46,XY; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TWINS;

ABNORMALITIES, MULTIPLE; ABORTION, EUGENIC; ADULT; CHROMOSOMES, HUMAN, PAIR 7; FATHERS; FEMALE; HEREDITY; HETEROZYGOTE; HOLOPROSENCEPHALY; HUMANS; MALE; PREGNANCY; PREGNANCY TRIMESTER, FIRST; PRENATAL DIAGNOSIS; SPECTRAL KARYOTYPING; TRANSLOCATION, GENETIC;

ERINACEIDAE;

EID: 0037329725     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/pd.552     Document Type: Article

References (12)

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